Objective Evaluation of Tubeless Thoracic Surgery in Early-Stage Lung Cancer Patients Using Multimodal Digital Device: A Prospective Study.
2/5 보강
TL;DR
Wearable-derived metrics showed modest variation, supporting feasibility rather than clinical superiority, while ePROs revealed differences suggesting tubeless surgery may offer a more favorable experience, validate a multimodal digital platform for perioperative assessment.
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
337 patients, 263 were enrolled and instructed to wear a wearable device and complete ePROs.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] We validated a multimodal digital platform for perioperative assessment. Wearable-derived metrics showed modest variation, supporting feasibility rather than clinical superiority, whereas ePROs revealed differences suggesting tubeless surgery may offer a more favorable experience.
OpenAlex 토픽 ·
Lung Cancer Diagnosis and Treatment
Tracheal and airway disorders
Social Media in Health Education
Wearable-derived metrics showed modest variation, supporting feasibility rather than clinical superiority, while ePROs revealed differences suggesting tubeless surgery may offer a more favorable exper
- p-value P < .001
APA
Runchen Wang, Qixia Wang, et al. (2026). Objective Evaluation of Tubeless Thoracic Surgery in Early-Stage Lung Cancer Patients Using Multimodal Digital Device: A Prospective Study.. The Annals of thoracic surgery, 121(5), 1202-1210. https://doi.org/10.1016/j.athoracsur.2025.09.008
MLA
Runchen Wang, et al.. "Objective Evaluation of Tubeless Thoracic Surgery in Early-Stage Lung Cancer Patients Using Multimodal Digital Device: A Prospective Study.." The Annals of thoracic surgery, vol. 121, no. 5, 2026, pp. 1202-1210.
PMID
41061814 ↗
Abstract 한글 요약
[BACKGROUND] Limited research has objectively assessed perioperative outcomes of tubeless thoracic surgery. This prospective study compared perioperative outcomes between tubeless and intubated surgery using a multimodal digital platform integrating a wearable device and electronic patient-reported outcomes (ePROs).
[METHODS] Of 337 patients, 263 were enrolled and instructed to wear a wearable device and complete ePROs. Propensity score matching (PSM) was applied to balance baseline characteristics.
[RESULTS] After PSM, 80 patients were included in each group. Compared with the intubation group, the tubeless group had shorter hospital length of stay (2.78 vs 3.91 days, P < .001), shorter chest tube duration (0.93 vs 2.26 days, P < .001), and lower drainage volume (128.90 vs 313.88 mL, P < .001). Wearable devices captured significant differences, with the tubeless group showing lower body temperature (36.68 °C vs 36.79 °C, P <.01) and heart rate (78.96 beats/min vs 85.23 beats/min, P < .001) on the second postoperative day. Oxygen saturation was higher in the tubeless group on postoperative day 1 (96.71% vs 95.95%, P < .001) and day 2 (96.39% vs 95.81%, P = .05). Sleep quality was better the day before (78.59 vs 75.74, P = .01) and on surgery day (85.48 vs 83.15, P < .001). ePROs reported less pain, coughing, dyspnea, and distress in the tubeless group.
[CONCLUSIONS] We validated a multimodal digital platform for perioperative assessment. Wearable-derived metrics showed modest variation, supporting feasibility rather than clinical superiority, whereas ePROs revealed differences suggesting tubeless surgery may offer a more favorable experience.
[METHODS] Of 337 patients, 263 were enrolled and instructed to wear a wearable device and complete ePROs. Propensity score matching (PSM) was applied to balance baseline characteristics.
[RESULTS] After PSM, 80 patients were included in each group. Compared with the intubation group, the tubeless group had shorter hospital length of stay (2.78 vs 3.91 days, P < .001), shorter chest tube duration (0.93 vs 2.26 days, P < .001), and lower drainage volume (128.90 vs 313.88 mL, P < .001). Wearable devices captured significant differences, with the tubeless group showing lower body temperature (36.68 °C vs 36.79 °C, P <.01) and heart rate (78.96 beats/min vs 85.23 beats/min, P < .001) on the second postoperative day. Oxygen saturation was higher in the tubeless group on postoperative day 1 (96.71% vs 95.95%, P < .001) and day 2 (96.39% vs 95.81%, P = .05). Sleep quality was better the day before (78.59 vs 75.74, P = .01) and on surgery day (85.48 vs 83.15, P < .001). ePROs reported less pain, coughing, dyspnea, and distress in the tubeless group.
[CONCLUSIONS] We validated a multimodal digital platform for perioperative assessment. Wearable-derived metrics showed modest variation, supporting feasibility rather than clinical superiority, whereas ePROs revealed differences suggesting tubeless surgery may offer a more favorable experience.
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